tert-Butyl 4-hydroxyphenethylcarbamate

97%

Reagent Code: #72782
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CAS Number 64318-28-1

science Other reagents with same CAS 64318-28-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.3 g/mol
Formula C₁₃H₁₉NO₃
thermostat Physical Properties
Melting Point 71-75°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a protective group for amines, particularly in peptide chemistry. It helps prevent unwanted reactions during complex multi-step synthesis processes. The tert-butyl group offers stability under various reaction conditions, while the carbamate linkage can be selectively removed when needed, making it a valuable tool in the development of pharmaceuticals and bioactive molecules. Additionally, its phenolic hydroxyl group can be further functionalized, enabling its use in the design of drug candidates or intermediates in medicinal chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97-100
Melting Point 71-75
Appearance Yellowish solid

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿300.00
1g
10-20 days ฿400.00
5g
10-20 days ฿1,160.00
25g
10-20 days ฿5,490.00
tert-Butyl 4-hydroxyphenethylcarbamate
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This compound is primarily utilized in organic synthesis as a protective group for amines, particularly in peptide chemistry. It helps prevent unwanted reactions during complex multi-step synthesis processes. The tert-butyl group offers stability under various reaction conditions, while the carbamate linkage can be selectively removed when needed, making it a valuable tool in the development of pharmaceuticals and bioactive molecules. Additionally, its phenolic hydroxyl group can be further functionalize

This compound is primarily utilized in organic synthesis as a protective group for amines, particularly in peptide chemistry. It helps prevent unwanted reactions during complex multi-step synthesis processes. The tert-butyl group offers stability under various reaction conditions, while the carbamate linkage can be selectively removed when needed, making it a valuable tool in the development of pharmaceuticals and bioactive molecules. Additionally, its phenolic hydroxyl group can be further functionalized, enabling its use in the design of drug candidates or intermediates in medicinal chemistry.

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